Your browser doesn't support javascript.
loading
Expression of immune response molecules and function of fas ligand on surface of AML WEHI-3 cells / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 535-538, 2006.
Artigo em Chinês | WPRIM | ID: wpr-233551
ABSTRACT
The purpose of this study was to investigate the expression of Fas, Fas ligand (FasL) and CD80 and function of FasL on the surface of acute myelomonocytic leukemia cells from WEHI-3 line. The expression of Fas, FasL and CD80 on the surface of WEHI-3 were detected by flow cytometry, the apoptosis of YAC-1 cell induced by FasL on the surface of WEHI-3 were detected by (3)H-TdR incorporation. The results showed that the expression rate of Fas, FasL and CD80 on the surface of WEHI-3 cells were (6.75 +/- 2.31)% (n = 5), (63.73 +/- 5.23)% (n = 5) and (5.06 +/- 0.41)% (n = 5) respectively. The apoptosis rate of YAC-1 cells (target cells) co-cultured with WEHI-3 cells (Effector cells) at the rate of 13, 110 and 130 were (26 +/- 4.5)%, (35 +/- 3.2)% and (43 +/- 2.7)% (n = 5) respectively. It is concluded that WEHI-3 cells have high expression of FasL and low expression of Fas and CD80 on their cell membrane, and can induce the apoptosis of Fas(+) YAC-1 cells.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Fisiologia / Células Tumorais Cultivadas / Leucemia Mielomonocítica Aguda / Membrana Celular / Apoptose / Antígeno B7-1 / Receptor fas / Proteína Ligante Fas / Metabolismo Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2006 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Fisiologia / Células Tumorais Cultivadas / Leucemia Mielomonocítica Aguda / Membrana Celular / Apoptose / Antígeno B7-1 / Receptor fas / Proteína Ligante Fas / Metabolismo Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2006 Tipo de documento: Artigo